Evidence map›Paper›PMID 41137622›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Comparison of amyloid chronicity and EYO in autosomal dominant Alzheimer's disease.

Julie K Wisch, Nicole S McKay, Matthew Zammit, Bradley T Christian, Stephanie A Schultz, Peter R Millar, Natalie S Ryan, David M Cash, Christopher R S Belder, Patricio Chrem and 21 more

Abstract readComparative Study
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Comparison of amyloid chronicity and EYO in autosomal dominant Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Julie K WischDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.ORCID 0000-0003-3624-2784
Nicole S McKayDepartment of Radiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Matthew ZammitDepartment of Medical Physics and Psychiatry, University of Wisconsin Madison, Madison, Wisconsin, USA.
Bradley T ChristianDepartment of Medical Physics and Psychiatry, University of Wisconsin Madison, Madison, Wisconsin, USA.
Stephanie A SchultzDepartment of Neurology, Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, USA.
Peter R MillarDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Natalie S RyanDepartment of Neurology, University College London, London, UK.
David M CashDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Christopher R S BelderDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Patricio ChremCentro de Memoria y Envejecimiento, Fundación Favaloro - Anexo Moreno, Calle Moreno, Argentin.
Carlos CruchagaHope Center for Neurological Disorders, Washington University in St. Louis, St. Louis, Missouri, USA.
Laura IbanezHope Center for Neurological Disorders, Washington University in St. Louis, St. Louis, Missouri, USA.
Mathias JuckerHertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Igor YakushevDept. of Nuclear Medicine, Klinikum rechts der Isar, Technical University of Munich (TUM), München, Germany.
Gregory S DayDepartment of Neurology, Mayo Clinic Florida - Jacksonville Campus, Jacksonville, Florida, USA.
Mei MurphyDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Jorge Llibre-GuerraDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
David AguillonGrupo de Neurociencias de Antioquia (GNA), Facultad de Medicina, Universidad de Antioquia, Sede de Investigación Universitaria (SIU), Medellín, Colombia.
Jee Hoon RohDepartments of Physiology & Neurology, College of Medicine, Korea University, Seoul , Republic of Korea.
Chengjie XiongDepartment of Biostatistics, Washington University in St. Louis, St. Louis, Missouri, USA.
Guoqiao WangDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Yan LiDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Suzanne E SchindlerDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Cliff JackDepartment of Radiology, Mayo Clinic - Mayo Building West, Rochester, Minnesota, USA.
Eric McDadeDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Randall J BatemanDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Tammie L S BenzingerDepartment of Radiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Beau M AncesDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Dominantly Inherited Alzheimer Networ
Tobey BetthauserDepartment of Medical Physics and Psychiatry, University of Wisconsin Madison, Madison, Wisconsin, USA.
Brian GordonDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.

Funding

Imaging CoreU19AG032438 · NIA · WASHINGTON UNIVERSITY · PI BATEMAN, RANDALL J · 2010 to 2025
$53.9M
Multi-cohort study of factors that influence Alzheimer's disease biomarker and dementia timingR01AG080766 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI TOBEY JAMES BETTHAUSER · 2023 to 2026
$3.1M
Identifying variations in gamma-secretase function that are critical determinants of clinical and biomarker progression of Autosomal Dominant Alzheimer's disease: From mechanism to clinical trialsK01AG084816 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Stephanie Schultz · 2024 to 2026
$387k
Comparing epigenetic, proteomic, and MRI aging clocks in sporadic and autosomal-dominant Alzheimer diseaseK01AG090753 · NIA · WASHINGTON UNIVERSITY · PI Peter R Millar · 2025 to 2026
$257k
Alzheimer's Association SG-20-690363-DIANGerman Center for Neurodegenerative Diseases (DZNE)Japan Agency for Medical Research and DevelopmentMinistry of Health & WelfareMinistry of Science and ICT RS-2024-00344521NIA NIH HHS K01 AG084816NIA NIH HHS K01 AG090753NIA NIH HHS R01 AG080766NIA NIH HHS U19 AG032438NIA NIH HHS U19AG032438Raul Carrea Institute for Neurological Research(FLENI)Spanish Institute of Health Carlos III (ISCIII)the Barnes-Jewish Hospital Foundationthe Charles F and Joanne Knight Alzheimer's Research Initiativethe Daniel J Brennan MD fundthe Hope Center for Neurological Disordersthe Mallinckrodt Institute ofRadiologythe Paula and Rodger Riney fundUKDementia Research Institute at University College London
6 · The paper itself

Abstract

introductionPreclinical Alzheimer's disease (AD) can be described relative to biomarker positivity onset time.

methodsWe estimated time from amyloid positivity (A+) using sampled iterative local approximation (SILA) in a longitudinal autosomal dominant AD (ADAD) sample (N = 379) with amyloid positron emission tomography. We compared (1) predicted age at A+ to imputed age, (2) estimated age at A+ to estimated age at symptom onset, and (3) variance in cognitive performance explained.

resultsMean error between imputed and SILA-estimated age at A+ (N = 26) was 1.15 years. Age at A+ explained 39% of estimated years to symptom onset (EYO) variance. Time from A+ explained 19% of cognitive composite variance and 14% of Clinical Dementia Rating Sum of Boxes CDR-SB variance; EYO explained 43% and 57%, respectively. DISCUSSION: SILA estimates A+ age in ADAD with reasonably good accuracy. SILA-estimated time from A+ describes the start of pathology, but the time from A+ onset to symptoms is variable in ADAD and better described by EYO. HIGHLIGHTS: Amyloid chronicity predicts a 14-year preclinical AD phase in ADAD. SILA accurately estimates age at A+ (MAE < 2 years). EYO outperforms chronicity in predicting symptom onset. APP mutation carriers show atypical amyloid accumulation. Chronicity models help reveal AD heterogeneity in preclinical stages.

Indexed as

Alzheimer DiseaseAmyloidAmyloid beta-PeptidesAgedAge of OnsetBiomarkersDisease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle AgedPositron-Emission TomographyAmyloidAmyloid beta-PeptidesBiomarkersAlzheimer's diseasebiomarkersgenetic causes of Alzheimer's diseasenumeric methods

Identifiers

PMID41137622
PMCPMC12552894

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.